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rs7807268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 2 1.4x risk for Crohn's disease
(C;G) 2 1.3x risk for Crohn's disease
(G;G) normal
ReferenceGRCh38 38.1/141
Chromosome7
Position148560956
is asnp
is mentioned by
dbSNPrs7807268
ebirs7807268
HLIrs7807268
Exacrs7807268
Varsomers7807268
Maprs7807268
PheGenIrs7807268
hapmaprs7807268
1000 genomesrs7807268
hgdprs7807268
ensemblrs7807268
gopubmedrs7807268
geneviewrs7807268
scholarrs7807268
googlers7807268
pharmgkbrs7807268
gwascentralrs7807268
openSNPrs7807268
23andMers7807268
23andMe allrs7807268
SNP Nexus

SNPshotrs7807268
SNPdbers7807268
MSV3drs7807268
GWAS Ctlgrs7807268
GMAF0.4931
Max Magnitude2
? (C;C) (C;G) (G;G) 28
rs7807268 has been reported in a large study to be associated with Crohn's disease.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.38 (CI 1.20-1.60), and for homozygotes, 1.47 (CI 1.24-1.74). [PMID 17554300OA-icon.png]

  • Note: there is a slight amount of ambiguity over the orientation of this SNP information relative to the dbSNP entry.


GET Evidence
rs7807268
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.507812
summary